haplotype were previously identified as susceptibility loci for narcolepsy with cataplexy. This study was conducted in order to investigate whether these genetic markers are associated with Japanese CNS hypersomnias (essential hypersomnia: EHS) other than narcolepsy with cataplexy. haplotype) was observed in EHS.CPT1B, CHKB and HLA are candidates for susceptibility to CNS hypersomnias (EHS), as well as narcolepsy with cataplexy
Narcolepsy is a neurological disorder characterized by excessive daytime sleepiness and cataplexy. T...
Narcolepsy is a rare sleep disorder with the strongest human leukocyte antigen (HLA) association eve...
Objectives: Polymorphisms in the TCRA and P2RY11, two immune related genes, are associated with narc...
Background: SNP rs5770917 located between CPT1B and CHKB, and HLA-DRB1*1501-DQB1*0602 haplotype were...
Essential hypersomnia (EHS), a sleep disorder characterized by excessive daytime sleepiness, can be ...
Background: The HLA-DQB1*06:02 allele across all ethnic groups and the rs5770917 variation between C...
Introduction. The determination of HLA class II genotype is widely used to confirm the diagnosis of ...
[[abstract]]Background: Narcolepsy is a rare, chronic, disabling neuropsychiatric disorder character...
Prior research has identified five common genetic variants associated with narcolepsy with cataplexy...
Prior research has identified five common genetic variants associated with narcolepsy with cataplexy...
Human narcolepsy-cataplexy, a sleep disorder associated with a centrally mediated hypocretin (orexin...
The purpose of this study was to investigate the association of human leukocyte antigen (HLA) class ...
Human narcolepsy is a hypersomnia that is affected by multiple genetic and environmental factors. On...
Introduction The determination of HLA class II genotype is widely used to confirm the diagnosis of ...
Narcolepsy is a unique model for dysfunction in mechanisms that regulate sleep and wakefulness. the ...
Narcolepsy is a neurological disorder characterized by excessive daytime sleepiness and cataplexy. T...
Narcolepsy is a rare sleep disorder with the strongest human leukocyte antigen (HLA) association eve...
Objectives: Polymorphisms in the TCRA and P2RY11, two immune related genes, are associated with narc...
Background: SNP rs5770917 located between CPT1B and CHKB, and HLA-DRB1*1501-DQB1*0602 haplotype were...
Essential hypersomnia (EHS), a sleep disorder characterized by excessive daytime sleepiness, can be ...
Background: The HLA-DQB1*06:02 allele across all ethnic groups and the rs5770917 variation between C...
Introduction. The determination of HLA class II genotype is widely used to confirm the diagnosis of ...
[[abstract]]Background: Narcolepsy is a rare, chronic, disabling neuropsychiatric disorder character...
Prior research has identified five common genetic variants associated with narcolepsy with cataplexy...
Prior research has identified five common genetic variants associated with narcolepsy with cataplexy...
Human narcolepsy-cataplexy, a sleep disorder associated with a centrally mediated hypocretin (orexin...
The purpose of this study was to investigate the association of human leukocyte antigen (HLA) class ...
Human narcolepsy is a hypersomnia that is affected by multiple genetic and environmental factors. On...
Introduction The determination of HLA class II genotype is widely used to confirm the diagnosis of ...
Narcolepsy is a unique model for dysfunction in mechanisms that regulate sleep and wakefulness. the ...
Narcolepsy is a neurological disorder characterized by excessive daytime sleepiness and cataplexy. T...
Narcolepsy is a rare sleep disorder with the strongest human leukocyte antigen (HLA) association eve...
Objectives: Polymorphisms in the TCRA and P2RY11, two immune related genes, are associated with narc...